CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this gene

A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD)

The solute carrier family 9 member A6 localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume

which are thought to be involved in protein-protein interactions

An important paralog of C1R is HP

CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this geneCEP68 (Centrosomal Protein 68) is a Protein Coding gene. Diseases associated with CEP68 include Retinitis Pigmentosa 28. Involved in maintenance of centrosome cohesion, probably as part of a linker structure which prevents centrosome splitting (PubMed: 18042621). Required for localization of CDK5RAP2 to the centrosome during interphase.